Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7786877 7 100616392 downstream gene variant A/G snv 0.22 2
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 6
rs4434553
TFR2
1.000 0.040 7 100642568 intron variant A/G snv 0.40 1
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs7383856
ACTL6B
7 100644788 intron variant G/A snv 4.9E-02 1
rs116979562
EPHB4
7 100816525 intron variant G/A snv 1.6E-02 2
rs6584485 10 102177487 intergenic variant C/T snv 0.76 1
rs2290707
RRM2B ; UBR5-AS1
8 102239027 upstream gene variant C/A snv 2.8E-02 2
rs4906190
ZNF839
14 102317171 upstream gene variant A/C;G;T snv 1
rs4900538
LOC105370680
14 102527728 intergenic variant T/A;C;G snv 2
rs2902548
SFXN2
10 102727625 intron variant C/T snv 0.18 0.20 1
rs200510190
CNNM2
10 103031838 intron variant C/- del 0.41 2
rs11160753 14 103541163 downstream gene variant C/G;T snv 1
rs7916093
LOC102724351
10 103958628 intergenic variant T/C snv 0.16 2
rs77926410
KLRC3
12 10415926 intron variant A/G snv 9.8E-02 1
rs56287436
SLC12A7
5 1080019 intron variant G/A snv 0.32 2
rs4237579
C11orf65
11 108408474 intron variant A/G snv 0.54 1
rs7943203
POGLUT3
11 108473354 3 prime UTR variant G/A snv 0.43 2
rs9521017
MYO16
13 108766811 intron variant G/T snv 0.32 2
rs11153147
ARMC2
6 108982855 downstream gene variant A/C;G snv 1
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs9374080
CCDC162P
6 109295217 intron variant T/C snv 0.40 1
rs13191948
CCDC162P
6 109313396 intron variant C/T snv 0.40 2
rs11966072
CCDC162P
6 109313625 intron variant A/G snv 0.26 4
rs61358232 13 109749719 downstream gene variant A/T snv 0.27 2